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Page 1
Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study.
Hugon-Rodin J, Carrière C, Claeyssens S, Trillot N, Drillaud N, Biron-Andreani C, Lavenu-Bombled C, Wieland A, Flaujac C, Stieltjes N, Lebreton A, Brungs T, Hegglin A, Fiore M, Desconclois C, Gay V, Tardy-Poncet B, Beurrier P, Barbay V, Chamouni P, Maistre E, Simurda T, Casini A. Hugon-Rodin J, et al. Among authors: lavenu bombled c. J Thromb Haemost. 2023 Aug;21(8):2126-2136. doi: 10.1016/j.jtha.2023.04.035. Epub 2023 May 11. J Thromb Haemost. 2023. PMID: 37172732
Pulmonary artery thrombosis during acute chest syndrome in sickle cell disease.
Mekontso Dessap A, Deux JF, Abidi N, Lavenu-Bombled C, Melica G, Renaud B, Godeau B, Adnot S, Brochard L, Brun-Buisson C, Galacteros F, Rahmouni A, Habibi A, Maitre B. Mekontso Dessap A, et al. Am J Respir Crit Care Med. 2011 Nov 1;184(9):1022-9. doi: 10.1164/rccm.201105-0783OC. Am J Respir Crit Care Med. 2011. PMID: 21836136
Clinical characteristics and laboratory testing of patients with suspected HIT: a survey on current practice in 11 university hospitals in France.
Bidet A, Tardy Poncet B, Desprez D, de Maistre E, Presles E, Lecompte T, Lavenu-Bombled C, Huisse MG, Wolf M, Morange P, Racadot E, Mouton C, Grunebaum L, Pouplard C, Tardy B; GEHT-HIT study group. Bidet A, et al. Thromb Res. 2010 Jun;125(6):e294-9. doi: 10.1016/j.thromres.2010.02.003. Epub 2010 Feb 23. Thromb Res. 2010. PMID: 20181380
High prevalence of the natural Asn89Asp mutation in the GP1BB gene associated with Bernard-Soulier syndrome in French patients from the genetic isolate of Reunion Island.
Fiore M, De Thoré C, Randrianaivo-Ranjatoelina H, Baas MJ, Jacquemont ML, Dreyfus M, Lavenu-Bombled C, Li R, Gachet C, Dupuis A, Lanza F. Fiore M, et al. Among authors: lavenu bombled c. Br J Haematol. 2020 May;189(3):e67-e71. doi: 10.1111/bjh.16479. Epub 2020 Jan 30. Br J Haematol. 2020. PMID: 31997307 Free PMC article. No abstract available.
32 results